(R)-tert-Butyl (1-(4-bromophenyl)-2-hydroxyethyl)carbamate

97%

Reagent Code: #37271
fingerprint
CAS Number 849178-85-4

science Other reagents with same CAS 849178-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.19 g/mol
Formula C₁₃H₁₈BrNO₃
badge Registry Numbers
MDL Number MFCD28148212
thermostat Physical Properties
Boiling Point 438.3±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a chiral intermediate for the production of pharmaceuticals and biologically active molecules. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and cancer. The tert-butyl carbamate group acts as a protective group for amines, allowing selective reactions to occur at other functional sites. Additionally, its chiral nature is crucial for synthesizing enantiomerically pure compounds, which are often required for effective and safe therapeutic agents. It is also employed in research settings for studying enzyme inhibition and receptor binding mechanisms due to its specific stereochemistry and functional groups.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,403.00
inventory 1g
10-20 days ฿11,700.00
inventory 250mg
10-20 days ฿4,329.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-tert-Butyl (1-(4-bromophenyl)-2-hydroxyethyl)carbamate
No image available

This compound is primarily utilized in organic synthesis as a chiral intermediate for the production of pharmaceuticals and biologically active molecules. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and cancer. The tert-butyl carbamate group acts as a protective group for amines, allowing selective reactions to occur at other functional sites. Additionally

This compound is primarily utilized in organic synthesis as a chiral intermediate for the production of pharmaceuticals and biologically active molecules. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and cancer. The tert-butyl carbamate group acts as a protective group for amines, allowing selective reactions to occur at other functional sites. Additionally, its chiral nature is crucial for synthesizing enantiomerically pure compounds, which are often required for effective and safe therapeutic agents. It is also employed in research settings for studying enzyme inhibition and receptor binding mechanisms due to its specific stereochemistry and functional groups.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...